Canonical Allele Identifier: CA2319221831

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2040891223
• gnomAD v4: 19-4094722-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094722A>G , CM000681.2:g.4094722A>G	GRCh38
NC_000019.9:g.4094720A>G , CM000681.1:g.4094720A>G	GRCh37
NC_000019.8:g.4045720A>G	NCBI36
NG_007996.1:g.34407T>C , LRG_750:g.34407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-224T>C
ENST00000688002.1:n.3198-224T>C
ENST00000688751.1:n.183-224T>C
ENST00000689792.1:n.951-224T>C
ENST00000262948.10:c.1047-224T>C MANE Select	ENSP00000262948.4:n.1047-224T>C
ENST00000262948.9:c.1047-224T>C	ENSP00000262948.3:n.1047-224T>C
ENST00000394867.8:c.756-224T>C	ENSP00000378336.1:n.756-224T>C
ENST00000597263.5:n.232-224T>C
ENST00000599021.1:c.157-224T>C
ENST00000600584.5:n.2272T>C
ENST00000601786.5:n.1348-224T>C
NM_030662.3:c.1047-224T>C , LRG_750t1:c.1047-224T>C	NP_109587.1:n.1047-224T>C
XM_006722799.2:c.768-224T>C	XP_006722862.1:n.768-224T>C
XM_011528133.1:c.477-224T>C	XP_011526435.1:n.477-224T>C
XM_017026989.1:c.1371T>C	XP_016882478.1:p.Pro457=
XM_017026990.1:c.1092T>C	XP_016882479.1:p.Pro364=
NM_030662.4:c.1047-224T>C MANE Select	NP_109587.1:n.1047-224T>C